Howard J. Jacob

1991–2025 年に発表

120
論文数
24,945
被引用数
82
h 指数
116
i10 指数

被引用数

Howard J. Jacob の年別被引用数1992 年: 被引用 13 件1993 年: 被引用 17 件1994 年: 被引用 31 件1995 年: 被引用 38 件1996 年: 被引用 50 件1997 年: 被引用 60 件1998 年: 被引用 79 件1999 年: 被引用 70 件2000 年: 被引用 106 件2001 年: 被引用 86 件2002 年: 被引用 167 件2003 年: 被引用 163 件2004 年: 被引用 175 件2005 年: 被引用 165 件2006 年: 被引用 156 件2007 年: 被引用 106 件2008 年: 被引用 124 件2009 年: 被引用 130 件2010 年: 被引用 138 件2011 年: 被引用 146 件2012 年: 被引用 162 件2013 年: 被引用 223 件2014 年: 被引用 215 件2015 年: 被引用 186 件2016 年: 被引用 157 件2017 年: 被引用 178 件2018 年: 被引用 174 件2019 年: 被引用 467 件2020 年: 被引用 488 件2021 年: 被引用 461 件2022 年: 被引用 456 件2023 年: 被引用 506 件2024 年: 被引用 1,129 件2025 年: 被引用 451 件2026 年: 被引用 16 件

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,345 件、この内訳の 29.2%中国: 引用元論文 1,306 件、この内訳の 11.4%イギリス: 引用元論文 960 件、この内訳の 8.4%ドイツ: 引用元論文 628 件、この内訳の 5.5%カナダ: 引用元論文 432 件、この内訳の 3.8%フランス: 引用元論文 397 件、この内訳の 3.4%オーストラリア: 引用元論文 327 件、この内訳の 2.8%イタリア: 引用元論文 318 件、この内訳の 2.8%オランダ: 引用元論文 299 件、この内訳の 2.6%日本: 引用元論文 297 件、この内訳の 2.6%スウェーデン: 引用元論文 261 件、この内訳の 2.3%フィンランド: 引用元論文 228 件、この内訳の 2%
0%29.2%その他 23.2%

分野

  • Biochemistry, Genetics and Molecular Biology58.5%
  • Medicine27.4%
  • Neuroscience3.7%
  • Immunology and Microbiology2.7%
  • Agricultural and Biological Sciences1.9%
  • Nursing1.7%
  • その他4.1%

トピック

  • Genetic Associations and Epidemiology5.3%
  • Genomics and Rare Diseases3.2%
  • Genetic Mapping and Diversity in Plants and Animals2.4%
  • Extracellular vesicles in disease2.3%
  • Bioinformatics and Genomic Networks2%
  • MicroRNA in disease regulation1.9%
  • その他82.9%

共著者

全論文

検索で開く
  1. FinnGen provides genetic insights from a well-phenotyped isolated population

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, FinnGen, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja ほか 69 名 - Nature 2023 被引用: 4,257

  2. Characterization of human plasma-derived exosomal RNAs by deep sequencing

    著者: , , , , , , , , , , , , , - BMC Genomics 2013 被引用: 1,067

  3. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Huy Nguyen, Cara Mason, Christopher Farnham, Charlotte Tolonen, Laura D. Gauthier, Namrata Gupta, Daniel G. MacArthur, Heidi L. Rehm, Cotton Seed, Anthony Philippakis, Mark J. Daly, J. Wade Davis, Heiko Runz, Melissa Miller, Benjamin M. Neale - Cell Genomics 2022 被引用: 295

  4. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt ほか 11 名 - Nature Genetics 2021 被引用: 427

  5. FinnGen: Unique genetic insights from combining isolated population and national health register data

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari, Mari Niemi, Marianna Niemi ほか 66 名 - medRxiv 2022 被引用: 412

  6. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael F. Wangler, Monte Westerfield, Matthew T. Wheeler, Anastasia L. Wise, Elizabeth A. Worthey, Shinya Yamamoto, Euan A. Ashley - New England Journal of Medicine 2018 被引用: 374

  7. Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ene Reimann, Bindu Swapna Madala, Tim R. Mercer, Chris Miller, Howard J. Jacob, Tiffany Truong, Ali Moshrefi, Aparna Natarajan, Ana Granat, Gary P. Schroth, Rasika Kalamegham, Eric Peters, Virginie Petitjean, Ashley Walton, Tsai-Wei Shen, Keyur Talsania, Cristobal Juan Vera, Kurt J. Langenbach, Maryellen de Mars, Jennifer Hipp, James C. Willey, Jing Wang, Jyoti Shetty, Yuliya Kriga, Arati Raziuddin, Bao Tran, Yuanting Zheng, Ying Yu, Margaret C. Cam, Parthav Jailwala, Cu Nguyen, Daoud Meerzaman, Qingrong Chen, Chunhua Yan, Ben Ernest, Urvashi Mehra, Roderick V. Jensen, Wendell Jones, Jian‐Liang Li, Brian N. Papas, Mehdi Pirooznia, Yunching Chen, Fayaz Seifuddin, Zhipan Li, Xue‐Lu Liu, Wolfgang Resch, Jingya Wang, Leihong Wu, Gökhan Yavaş, Corey J. Miles, Baitang Ning, Weida Tong, Christopher E. Mason, Eric Donaldson, Samir Lababidi, Louis M. Staudt, Živana Težak, Huixiao Hong, Charles Wang, Leming Shi - Nature Biotechnology 2021 被引用: 213

  8. Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Satu Wedenoja, Satu Leminen, Aija Lähdesmäki, Susanna Mehtälä, Christina Salmén, Aarno Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Athena Matakidou, Adam Platt, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Robert M. Plenge, Joseph Maranville, Mark I. McCarthy, Julie Hunkapiller, Margaret G. Ehm, Kirsi Auro, Simonne Longerich, Caroline S. Fox, Anders Mälarstig, K. Klinger, Deepak Raipal, Eric Green, Robert Graham, Robert Yang, Chris O ́Donnell, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Jari A. Laukkanen, Marco Hautalahti, Outi Tuovila, Raimo Pakkanen, Jeffrey F. Waring, Bridget Riley‐Gillis, Fedik Rahimov, Ioanna Tachmazidou, Chia‐Yen Chen, Zhihao Ding, Marc Jung, Shameek Biswas, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Arto Mannermaa ほか 259 名 - JAMA Cardiology 2023 被引用: 131

  9. The role of polygenic risk and susceptibility genes in breast cancer over the course of life

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mervi Aavikko, Mitja Kurki, Oluwaseun Alexander Dada, Pietro Della Briotta Parolo, Risto Kajanne, Sina Rüeger, Susanna Lemmelä, Taru Tukiainen, Tiinamaija Tuomi, Timo P. Sipilä, Tuomo Kiiskinen, Vincent Llorens, Adam Ziemann, Anne Lehtonen, Apinya Lertratanakul, Bob Georgantas, Bridget Riley‐Gillis, Danjuma Quarless, Fedik Rahimov, Howard J. Jacob, Jeffrey F. Waring, J. Wade Davis, Nizar Smaoui, Relja Popovic, Sahar Esmaeeli, Athena Matakidou, Ben Challis, David A. Close, Eleonor Wigmore, Slavé Petrovski, Chia‐Yen Chen, Ellen Tsai, Heiko Runz, Jimmy Z. Liu, Paola G. Bronson, Sally John, Sanni Lahdenperä, Stephanie Loomis, Susan Eaton, Yunfeng Huang, Erika Kvikstad, Minal Çalışkan, Samir Wadhawan, Elmutaz Shaikho Elhaj Mohammed, Janet van Adelsberg, Joseph Maranville, Marla Hochfeld, Robert M. Plenge, Shameek Biswas, Steven M. Greenberg, Andrew S. Peterson, David F. Choy, Diana Chang, Edmond Teng, Erich C. Strauss, Geoff Kerchner, Hao Chen, Hubert Chen, Jennifer L. Schutzman, John A. Michon, Julie Hunkapiller, Mark I. McCarthy, Natalie Bowers, Sarah A. Pendergrass, Tushar Bhangale, David Pulford, Dawn Waterworth, Diptee Kulkarni, Fanli Xu, Jo Betts ほか 180 名 - Nature Communications 2020 被引用: 173

  10. Systematic single-variant and gene-based association testing of thousands of phenotypes in 426,370 UK Biobank exomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Huy Nguyen, Cara Mason, Christopher Farnham, Charlotte Tolonen, Laura D. Gauthier, Namrata Gupta, Daniel G. MacArthur, Heidi L. Rehm, Cotton Seed, Anthony Philippakis, Mark J. Daly, J. Wade Davis, Heiko Runz, Melissa Miller, Benjamin M. Neale - medRxiv 2021 被引用: 62

  11. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arto Lehistö, Elina Kilpeläinen, Georg Brein, Awaisa Ghazal, Jarmo Harju, Kalle Pärn, Pietro Della Briotta Parolo, Risto Kajanne, Susanna Lemmelä, Timo P. Sipilä, Tuomas Sipilä, Ulrike Lyhs, Vincent Llorens, Teemu Niiranen, Kati Kristiansson, Lotta Männikkö, Manuel González Jiménez, Markus Perola, Regis Wong, Terhi Kilpi, Tero Hiekkalinna, Elina Järvensivu, Essi Kaiharju, Hannele Mattsson, Markku Laukkanen, Päivi Laiho, Sini Lähteenmäki, Tuuli Sistonen, Sirpa Soini, Adam Ziemann, Anne Lehtonen, Apinya Lertratanakul, Bob Georgantas, Bridget Riley‐Gillis, Danjuma Quarless, Fedik Rahimov, Graham Heap, Howard J. Jacob, Jeffrey F. Waring, J. Wade Davis, Nizar Smaoui, Relja Popovic, Sahar Esmaeeli, Jeff Waring, Athena Matakidou, Ben Challis, David A. Close, Slavé Petrovski, Antti Karlsson, Johanna Schleutker, Kari Pulkki, Petri Virolainen, Lila Kallio, Arto Mannermaa, Sami Heikkinen, Veli‐Matti Kosma, Chia‐Yen Chen, Heiko Runz, Jimmy Liu, Paola G. Bronson, Sally John, Sanni Lahdenperä, Susan Eaton, Wei Zhou, Minna Hendolin, Outi Tuovila, Raimo Pakkanen, Joseph Maranville, Keith Usiskin, Marla Hochfeld ほか 161 名 - Nature Communications 2019 被引用: 195

  12. The Collaborative Cross, a community resource for the genetic analysis of complex traits

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Doug Matthews, Melloni N. Cook, Roger Cox, John C. Crabbe, Wim E. Crusio, Ariel Darvasi, Christian F. Deschepper, Bastien Llamas, R. W. Doerge, Charles R. Farber, Juan F. Medrano, Jiřı́ Forejt, Daniel P. Gaile, Steven J. Garlow, Hartmut Geiger, Howard K. Gershenfeld, Terry Gordon, Weikuan Gu, Gerald de Haan, Richard S. Nowakowski, Nancy L. Hayes, Craig Heller, Heinz Himmelbauer, Kent W. Hunter, Hui-Chen Hsu, Fuad A. Iraqi, Boris Ivandic, Howard J. Jacob, Ritsert C. Jansen, Karl J. Jepsen, Dabney K. Johnson, Gerd Kempermann, Christina Kendziorski, Malak Kotb, R. Frank Kooy, Frank Lammert, Jean‐Michel Lassalle, Pedro R. Löwenstein, Aldons J. Lusis, Kenneth F. Manly, Ralph Marcucio, Darla R. Miller, Beverly A. Mock, Jeffrey S. Mogil, Xavier Montagutelli, Grant Morahan, D.G. Morris, Richard Mott, William Valdar, Joseph H. Nadeau, Hiroki Nagase, Bruce F. O’Hara, А. В. Осадчук, Nengjun Yi, Grier P. Page, Abraham A. Palmer, Leena Peltonen-Palotie, Daniel Pomp, Daniel Pomp, Michal Pravenec, Daniel R. Prows, Zhonghua Qi, Roger H. Reeves, John Roder, Glenn D. Rosen, Eric E. Schadt, Leonard C. Schalkwyk, Ze’ev Seltzer, Kazuhiro Shimomura, Siming Shou ほか 13 名 - Nature Genetics 2004 被引用: 1,193

  13. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Athena Matakidou, Heiko Runz, Sally John, Robert M. Plenge, Mark I. McCarthy, Julie Hunkapiller, Meg Ehm, Dawn Waterworth, Caroline S. Fox, Anders Mälarstig, Kathy Klinger, Kathy Call, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Kari Pulkki, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Riitta Kaarteenaho, Seppo Vainio, Kimmo Savinainen, Veli‐Matti Kosma, Urho M. Kujala, Other experts and non-voting members, Outi Tuovila, Minna Hendolin, Raimo Pakkanen, Pharmaceutical companies, Jeff Waring, Bridget Riley‐Gillis, Athena Matakidou, Heiko Runz, Jimmy Z. Liu, Shameek Biswas, Julie Hunkapiller, Dawn Waterworth, Meg Ehm, Dorothée Diogo, Caroline S. Fox, Anders Mälarstig, Catherine Marshall, Xinli Hu, Kathy Call, Kathy Klinger, Matthias Gossel, Samuli Ripatti, Johanna Schleutker, Markus Perola, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Reijo Laaksonen, Arto Mannermaa, Urho M. Kujala, Other experts and non-voting members, Outi Tuovila, Minna Hendolin, Raimo Pakkanen, Neurology group, Hilkka Soininen, Valtteri Julkunen, Anne M. Remes, Reetta Kälviäinen, Mikko Hiltunen, Jukka Peltola, Pentti J. Tienari, Juha O. Rinne ほか 332 名 - Nature 2020 被引用: 148

  14. Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, FinnGen, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja ほか 69 名 - Nature 2023 被引用: 121

  15. Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid - medRxiv 2020 被引用: 96

  16. The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases

    著者: , , , , , , , , , - BMC Medical Genomics 2022 被引用: 83

  17. Knockout Rats via Embryo Microinjection of Zinc-Finger Nucleases

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2009 被引用: 927

  18. Rats!

    著者: , - Disease Models & Mechanisms 2009 被引用: 242

  19. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fabio Pizza, Monica Moresco, Catherine Crowe, Stephen K. Van Den Eeden, Michel Lecendreux, Patrice Bourgin, Takashi Kanbayashi, F Martínez-Orozco, Rosa Peraita‐Adrados, Antonio Benetó, Jacques Montplaisir, Alex Désautels, Yu‐Shu Huang, FinnGen, Thomas D. Als, Adam Ziemann, Ali Abbasi, Anne Lehtonen, Apinya Lertratanakul, Bridget Riley‐Gillis, Fedik Rahimov, Howard J. Jacob, Jeffrey F. Waring, Mengzhen Liu, Nizar Smaoui, Relja Popovic, Adam Platt, Athena Matakidou, Benjamin Challis, Dirk S. Paul, Glenda Lassi, Ioanna Tachmazidou, Antti Hakanen, Johanna Schleutker, Nina Pitkänen, Perttu Terho, Petri Virolainen, Arto Mannermaa, Veli‐Matti Kosma, Chia‐Yen Chen, Heiko Runz, Sally John, Sanni Lahdenperä, Stephanie Loomis, Susan Eaton, George Okafo, Heli Salminen‐Mankonen, Marc Jung, Nathan Lawless, Zhihao Ding, Joseph Maranville, Marla Hochfeld, Robert M. Plenge, Shameek Biswas, Masahiro Kanai, Mutaamba Maasha, Wei Zhou, Outi Tuovila, Raimo Pakkanen, Jari A. Laukkanen, Teijo Kuopio, Kristiina Aittomäki, Antti Mäkitie, Natalia Pujol, Triin Laisk, Katriina Aalto‐Setälä, Johanna Mäkelä, Marco Hautalahti, Sarah Smith, Tom Southerington ほか 312 名 - Nature Communications 2023 被引用: 61

  20. Comparative Recombination Rates in the Rat, Mouse, and Human Genomes

    著者: , , , , , , , , - Genome Research 2004 被引用: 567

  21. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Katherine R. Chao, Gary Clark, Joy D. Cogan, Cynthia M. Cooper, William J. Craigen, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, David D. Draper, Annika M. Dries, David J. Eckstein, Lisa Emrick, Christine M. Eng, Cecilia Esteves, Tyra Estwick, Paul G. Fisher, Trevor S. Frisby, Kate Frost, William A. Gahl, Valerie Gartner, Rena A. Godfrey, Mitchell Goheen, Gretchen Golas, David Goldstein, Mary “Gracie” G. Gordon, Sarah E. Gould, Jean-Philippe F. Gourdine, Brett H. Graham, Catherine Groden, Andrea Gropman, Mary E. Hackbarth, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Isabel Hardee, Matthew Herzog, Ingrid A. Holm, Ellen M. Howerton, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Alanna E. Koehler, David M. Koeller, Isaac S. Kohane, Jennefer N. Kohler, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Jennifer Kyle, Seema R. Lalani, Lea Latham, Yvonne L. Latour, C. Christopher Lau, Jozef Lazar, Brendan Lee, Hane Lee, Paul R. Lee, Shawn Levy ほか 87 名 - The American Journal of Human Genetics 2017 被引用: 223

  22. The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lauren C. Briere, Donna M. Brown, Catherine A. Brownstein, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Katherine R. Chao, Gary Clark, Joy D. Cogan, Cynthia M. Cooper, William J. Craigen, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, David D. Draper, Annika M. Dries, Rachel L. Eastwood, David J. Eckstein, Lisa Emrick, Christine M. Eng, Cecilia Esteves, Tyra Estwick, Paul G. Fisher, Trevor S. Frisby, Kate Frost, William A. Gahl, Valerie Gartner, Rena A. Godfrey, Mitchell Goheen, Gretchen Golas, David B. Goldstein, Mary “Gracie” G. Gordon, Sarah E. Gould, Jean-Philippe F. Gourdine, Brett H. Graham, Catherine Groden, Andrea Gropman, Mary E. Hackbarth, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Isabel Hardee, Matthew Herzog, Ingrid A. Holm, Ellen M. Howerton, Brenda Iglesias, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Alanna E. Koehler, David M. Koeller, Isaac S. Kohane, Jennefer N. Kohler, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Jennifer Kyle, Seema R. Lalani, Lea Latham, Yvonne L. Latour, C. Christopher Lau, Jozef Lazar ほか 92 名 - The American Journal of Human Genetics 2017 被引用: 188

  23. Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Arto Mannermaa, Jari Laukkanen, Marco Hautalahti, Other Experts/Non-Voting Members, Outi Tuovila, Raimo Pakkanen, Pharmaceutical companies, Jeffrey Waring, Ioanna Tachmazidou, Chia-Yen Chen, Shameek Biswas, Zhihao Ding, Marc Jung, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Samuli Ripatti, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Katriina Aalto‐Setälä, Mika Kähönen, Johanna Mäkelä, Neurology Group, Reetta Kälviäinen, Valtteri Julkunen, Hilkka Soininen, Anne M. Remes, Mikko Hiltunen, Jukka Peltola, Pentti J. Tienari, Juha O. Rinne, Roosa Kallionpää, Ali Abbasi, Adam Ziemann, Sahar Esmaeeli, Nizar Smaoui, Anne Lehtonen, Susan Eaton, Sanni Lahdenperä, Janet van Adelsberg, Natalie Bowers, Edmond Teng, Sarah A. Pendergrass, Onuralp Söylemez, Kari Linden, Fanli Xu, Laura Addis, John D. Eicher ほか 290 名 - Communications Biology 2022 被引用: 51

  24. Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gabriel F. Batzli, Alan H. Beggs, Babak Behnam, Anna Bican, David Bick, Camille L. Birch, Devon Bonner, Braden Boone, Bret L. Bostwick, Lauren C. Briere, Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Shan Chen, Gary Clark, Terra R. Coakley, Joy D. Cogan, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Precilla D’Souza, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Ani Dillon, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, Emilie D. Douine, David D. Draper, David J. Eckstein, Lisa Emrick, Christine M. Eng, Ascia Eskin, Cecilia Esteves, Tyra Estwick, Carlos R. Ferreira, Brent L. Fogel, Noah D. Friedman, William A. Gahl, Emily Glanton, Rena A. Godfrey, David B. Goldstein, Sarah E. Gould, Jean-Philippe F. Gourdine, Catherine Groden, Andrea Gropman, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Matthew Herzog, Ingrid A. Holm, Jason Hom, Ellen M. Howerton, Yong Huang, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Isaac S. Kohane, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Seema R. Lalani, C. Christopher Lau ほか 116 名 - The American Journal of Human Genetics 2018 被引用: 107